BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 33948880)

  • 1. DOCK8-related Immunodeficiency Syndrome (DIDS): Report of Novel Mutations in Iranian Patients.
    Yousefnezhad S; Gharesouran J; Ghafouri-Fard S; Hosseinzadeh H; Ahmadian-Heris J; Jafari-Rouhi AH; Taheri M; Rezazadeh M
    J Mol Neurosci; 2021 Dec; 71(12):2456-2461. PubMed ID: 33948880
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DOCK8 mutation diagnosed using whole-exome sequencing of the dried blood spot-derived DNA: a case report of an Iraqi girl diagnosed in Japan.
    Al-Kzayer LFY; Al-Aradi HMH; Shigemura T; Sano K; Tanaka M; Hamada M; Ali KH; Aldaghir OM; Nakazawa Y; Okuno Y
    BMC Med Genet; 2019 Jun; 20(1):114. PubMed ID: 31242861
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome-first Approach Identified Novel Homozygous Dedicator of Cytokinesis 8 (DOCK8) Mutations in Three Unrelated Iranian Pedigrees Suspected with Hyper-IgE Syndrome.
    Aghebati-Maleki A; Shahani T; Momen T; Alyasin S; Changi-Ashtiani M; Biglari A; Shahrooei M; Javanian AS; Amini S; Bossuyt X; Rokni-Zadeh H
    Iran J Allergy Asthma Immunol; 2020 Apr; 19(2):193-199. PubMed ID: 32372632
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.
    Engelhardt KR; McGhee S; Winkler S; Sassi A; Woellner C; Lopez-Herrera G; Chen A; Kim HS; Lloret MG; Schulze I; Ehl S; Thiel J; Pfeifer D; Veelken H; Niehues T; Siepermann K; Weinspach S; Reisli I; Keles S; Genel F; Kutukculer N; Camcioğlu Y; Somer A; Karakoc-Aydiner E; Barlan I; Gennery A; Metin A; Degerliyurt A; Pietrogrande MC; Yeganeh M; Baz Z; Al-Tamemi S; Klein C; Puck JM; Holland SM; McCabe ER; Grimbacher B; Chatila TA
    J Allergy Clin Immunol; 2009 Dec; 124(6):1289-302.e4. PubMed ID: 20004785
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Autosomal recessive hyper-IgE syndrome caused by DOCK8 gene mutation with new clinical features: a case report.
    Yang J; Liu Y
    BMC Neurol; 2021 Jul; 21(1):288. PubMed ID: 34301197
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.
    Engelhardt KR; Gertz ME; Keles S; Schäffer AA; Sigmund EC; Glocker C; Saghafi S; Pourpak Z; Ceja R; Sassi A; Graham LE; Massaad MJ; Mellouli F; Ben-Mustapha I; Khemiri M; Kilic SS; Etzioni A; Freeman AF; Thiel J; Schulze I; Al-Herz W; Metin A; Sanal Ö; Tezcan I; Yeganeh M; Niehues T; Dueckers G; Weinspach S; Patiroglu T; Unal E; Dasouki M; Yilmaz M; Genel F; Aytekin C; Kutukculer N; Somer A; Kilic M; Reisli I; Camcioglu Y; Gennery AR; Cant AJ; Jones A; Gaspar BH; Arkwright PD; Pietrogrande MC; Baz Z; Al-Tamemi S; Lougaris V; Lefranc G; Megarbane A; Boutros J; Galal N; Bejaoui M; Barbouche MR; Geha RS; Chatila TA; Grimbacher B
    J Allergy Clin Immunol; 2015 Aug; 136(2):402-12. PubMed ID: 25724123
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel DOCK8 gene mutations lead to absence of protein expression in patients with hyper-IgE syndrome.
    Qin T; An Y; Liu C; Wu J; Dai R; Liu D; Li X; Jiang L; Wu D; Tang X; Song W; Wang T; Zhao X
    Immunol Res; 2016 Feb; 64(1):260-71. PubMed ID: 26659092
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel hemizygous CD40L mutation of X-linked hyper IgM syndromes and compound heterozygous DOCK8 mutations of hyper IgE syndromes in two Chinese families.
    Guo M; Ma Y; Cai K; Liu X; Liu W; Wang F; Qu N; Liu S
    Immunogenetics; 2024 Jun; 76(3):165-173. PubMed ID: 38587548
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutation in DOCK8-HIES with severe phenotype and successful transplantation.
    Al Shekaili L; Sheikh F; Al Gazlan S; Al Dhekri H; Al Mousa H; Al Ghonaium A; Al Saud B; Al Mohsen S; Rehan Khaliq AM; Al Sumayli S; Al Zahrani M; Dababo A; AlKawi A; Hawwari A; Arnaout R
    Clin Immunol; 2017 May; 178():39-44. PubMed ID: 27890707
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole Genome Sequencing Reveals a Chromosome 9p Deletion Causing DOCK8 Deficiency in an Adult Diagnosed with Hyper IgE Syndrome Who Developed Progressive Multifocal Leukoencephalopathy.
    Day-Williams AG; Sun C; Jelcic I; McLaughlin H; Harris T; Martin R; Carulli JP
    J Clin Immunol; 2015 Jan; 35(1):92-6. PubMed ID: 25388448
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cutaneous manifestations of DOCK8 deficiency syndrome.
    Chu EY; Freeman AF; Jing H; Cowen EW; Davis J; Su HC; Holland SM; Turner ML
    Arch Dermatol; 2012 Jan; 148(1):79-84. PubMed ID: 21931011
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The first cohort of Iranian patients with hyper immunoglobulin E syndrome: A long-term follow-up and genetic analysis.
    Tavassoli M; Abolhassani H; Yazdani R; Ghadami M; Azizi G; Abdolrahim Poor Heravi S; Moeini Shad T; Kokabee M; Movahedi M; Abdshahzadeh H; Gharagozlou M; Rezaei N; Esmaeilzadeh H; Aleyasin S; Aghamohammadi A
    Pediatr Allergy Immunol; 2019 Jun; 30(4):469-478. PubMed ID: 30801830
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE.
    Kienzler AK; van Schouwenburg PA; Taylor J; Marwah I; Sharma RU; Noakes C; Thomson K; Sadler R; Segal S; Ferry B; Taylor JC; Blair E; Chapel H; Patel SY
    Clin Immunol; 2016 Feb; 163():17-21. PubMed ID: 26680607
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical, immunological and molecular profiles of DOCK8 deficiency in six patients from a tertiary care centre in North India.
    Kumar Jindal A; Sil A; Aggarwal R; Tyagi R; Mondal S; Singh A; Barman P; Chawla S; Loganathan SK; Gupta K; Vinay K; Mahajan R; Saikia B; Kaur G; Sharma R; Saka R; Bhatia A; Sankhyan N; Pandiarajan V; Pilania R; Dhaliwal M; Sharma S; Vyas S; Suri D; Rawat A; Singh S
    Clin Exp Dermatol; 2024 Feb; 49(3):226-234. PubMed ID: 37815217
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel Variants of DOCK8 Deficiency in a Case Series of Iranian Patients.
    Momtazmanesh S; Rayzan E; Zoghi S; Shahkarami S; Molatefi R; Mohammadzadeh I; Ghaffari J; Mahmoudi H; Dmytrus J; Segarra-Roca A; Somekh I; Witzel M; Hauck F; Boztug K; Klein C; Rezaei N
    Endocr Metab Immune Disord Drug Targets; 2022; 22(1):159-168. PubMed ID: 33634762
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel large deletion of the DOCK8 gene in a Chinese family with autosomal-recessive hyper-IgE syndrome.
    Xue L; Yang Y; Wang S
    J Eur Acad Dermatol Venereol; 2015 Mar; 29(3):599-601. PubMed ID: 24673638
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DOCK8 Deficiency Presenting as an IPEX-Like Disorder.
    Alroqi FJ; Charbonnier LM; Keles S; Ghandour F; Mouawad P; Sabouneh R; Mohammed R; Almutairi A; Chou J; Massaad MJ; Geha RS; Baz Z; Chatila TA
    J Clin Immunol; 2017 Nov; 37(8):811-819. PubMed ID: 29058101
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis.
    Saettini F; Fazio G; Moratto D; Galbiati M; Zucchini N; Ippolito D; Dinelli ME; Imberti L; Mauri M; Melzi ML; Bonanomi S; Gerussi A; Pinelli M; Barisani C; Bugarin C; Chiarini M; Giacomelli M; Piazza R; Cazzaniga G; Invernizzi P; Giliani SC; Badolato R; Biondi A
    Front Immunol; 2021; 12():673487. PubMed ID: 33936120
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical, immunological, and genetic description of a Mexican cohort of patients with DOCK8 deficiency.
    Liquidano-Perez E; Maza-Ramos G; Perez Arias BA; Lugo Reyes SO; Barragan Arevalo T; Solorzano-Morales SA; Venegas Montoya E; Staines-Boone AT; Guzmán Cotaya R; Okada S; Picard C; Patin E; Ramirez-Uribe N; Bustamante-Ogando JC; Scheffler-Mendoza SC; Yamazaki-Nakashimada MA; Saez-de-Ocariz M; Espinosa Padilla SE; Gonzalez-Serrano ME
    Pediatr Allergy Immunol; 2024 Feb; 35(2):e14073. PubMed ID: 38351896
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8.
    Tangye SG; Gray PE; Pillay BA; Yap JY; Figgett WA; Reeves J; Kummerfeld SK; Stoddard J; Uzel G; Jing H; Su HC; Campbell DE; Sullivan A; Burnett L; Peake J; Ma CS
    J Clin Immunol; 2022 Jan; 42(1):119-129. PubMed ID: 34657245
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.